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<strong>The</strong> stra<strong>in</strong>s highlighted with alignment <strong>in</strong> <strong>the</strong> residual 364bp were analysed to assess<br />

if <strong>the</strong> sequence was part <strong>of</strong> a genomic island. <strong>The</strong> genomic island <strong>in</strong> C. koseri has<br />

yet to be identified <strong>in</strong> <strong>the</strong> literature or by a database. <strong>The</strong> genomic island, if present,<br />

did not share a conserved D flank with E. coli after an extension <strong>of</strong> 5kb <strong>in</strong> any <strong>of</strong> <strong>the</strong><br />

sequenced E. coli stra<strong>in</strong>s. <strong>The</strong> Salmonella stra<strong>in</strong>s all have def<strong>in</strong>ed and related<br />

pathogenicity islands associated with <strong>the</strong> leuX tRNA site (Table 3-6), functionally<br />

described as pathogencity islands conta<strong>in</strong><strong>in</strong>g <strong>the</strong> sefA-R chaperone-usher fimbrial<br />

operon.<br />

Salmonella stra<strong>in</strong> Size GC% Name<br />

Paratyphi A 31.4kb 47.20% -<br />

CT18 32.9kb 46.60% SPI-10<br />

Ty2 32.7kb 46.60% -<br />

Table 3-6 Pathogencity islands def<strong>in</strong>ed with<strong>in</strong> Salmonella stra<strong>in</strong>s that are leuX-associated<br />

<strong>in</strong>formation ga<strong>the</strong>red from Pathogenicity island database (Yoon et al. 2007)<br />

A second SGSP amplicon was generated from <strong>the</strong> EcoRV genomic library <strong>of</strong> E. coli<br />

E105 us<strong>in</strong>g <strong>the</strong> leuX D primer and <strong>the</strong> T3 universal primer. Sequenc<strong>in</strong>g was<br />

performed us<strong>in</strong>g <strong>the</strong> KS universal primer and resulted <strong>in</strong> 750bp <strong>of</strong> DNA sequence<br />

data. <strong>The</strong> results are depicted <strong>in</strong> Figure 3-14. Alignment <strong>of</strong> <strong>the</strong> full length sequence<br />

(bases 1-750) to <strong>the</strong> D flank <strong>of</strong> a number <strong>of</strong> sequenced E. coli stra<strong>in</strong>s (≥ 97%<br />

identity) as shown <strong>in</strong> Table 3-7.<br />

E. coli stra<strong>in</strong>s Score Expected value Identity<br />

UTI89 1315 0 98%<br />

APEC O1 1315 0 98%<br />

536 1315 0 98%<br />

E24377A 1279 0 97%<br />

Table 3-7 <strong>The</strong> highest scor<strong>in</strong>g sequences from <strong>the</strong> nucleotide sequence database based on<br />

nucleotide alignment (blastn)<br />

73

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